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Immune cell infiltrates as prognostic biomarkers in pancreatic ductal adenocarcinoma: a systematic review and meta‐analysis
Immune cell infiltration has been identified as a prognostic biomarker in several cancers. However, no immune based biomarker has yet been validated for use in pancreatic ductal adenocarcinoma (PDAC). We undertook a systematic review and meta‐analysis of immune cell infiltration, measured by immunoh...
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Published in: | The journal of pathology. Clinical research 2021-03, Vol.7 (2), p.99-112 |
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description | Immune cell infiltration has been identified as a prognostic biomarker in several cancers. However, no immune based biomarker has yet been validated for use in pancreatic ductal adenocarcinoma (PDAC). We undertook a systematic review and meta‐analysis of immune cell infiltration, measured by immunohistochemistry (IHC), as a prognostic biomarker in PDAC. All other IHC prognostic biomarkers in PDAC were also summarised. MEDLINE, EMBASE and Web of Science were searched between 1998 and 2018. Studies investigating IHC biomarkers and prognosis in PDAC were included. REMARK score and Newcastle–Ottawa scale were used for qualitative analysis. Random‐effects meta‐analyses were used to pool results, where possible. Twenty‐six articles studied immune cell infiltration IHC biomarkers and PDAC prognosis. Meta‐analysis found high infiltration with CD4 (hazard ratio [HR] = 0.65, 95% confidence interval [CI] = 0.51–0.83.) and CD8 (HR = 0.68, 95% CI = 0.55–0.84.) T‐lymphocytes associated with better disease‐free survival. Reduced overall survival was associated with high CD163 (HR = 1.62, 95% CI = 1.03–2.56). Infiltration of CD3, CD20, FoxP3 and CD68 cells, and PD‐L1 expression was not prognostic. In total, 708 prognostic biomarkers were identified in 1101 studies. In summary, high CD4 and CD8 infiltration are associated with better disease‐free survival in PDAC. Increased CD163 is adversely prognostic. Despite the publication of 708 IHC prognostic biomarkers in PDAC, none has been validated for clinical use. Further research should focus on reproducibility of prognostic biomarkers in PDAC in order to achieve this. |
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However, no immune based biomarker has yet been validated for use in pancreatic ductal adenocarcinoma (PDAC). We undertook a systematic review and meta‐analysis of immune cell infiltration, measured by immunohistochemistry (IHC), as a prognostic biomarker in PDAC. All other IHC prognostic biomarkers in PDAC were also summarised. MEDLINE, EMBASE and Web of Science were searched between 1998 and 2018. Studies investigating IHC biomarkers and prognosis in PDAC were included. REMARK score and Newcastle–Ottawa scale were used for qualitative analysis. Random‐effects meta‐analyses were used to pool results, where possible. Twenty‐six articles studied immune cell infiltration IHC biomarkers and PDAC prognosis. Meta‐analysis found high infiltration with CD4 (hazard ratio [HR] = 0.65, 95% confidence interval [CI] = 0.51–0.83.) and CD8 (HR = 0.68, 95% CI = 0.55–0.84.) T‐lymphocytes associated with better disease‐free survival. Reduced overall survival was associated with high CD163 (HR = 1.62, 95% CI = 1.03–2.56). Infiltration of CD3, CD20, FoxP3 and CD68 cells, and PD‐L1 expression was not prognostic. In total, 708 prognostic biomarkers were identified in 1101 studies. In summary, high CD4 and CD8 infiltration are associated with better disease‐free survival in PDAC. Increased CD163 is adversely prognostic. Despite the publication of 708 IHC prognostic biomarkers in PDAC, none has been validated for clinical use. Further research should focus on reproducibility of prognostic biomarkers in PDAC in order to achieve this.</description><identifier>ISSN: 2056-4538</identifier><identifier>EISSN: 2056-4538</identifier><identifier>DOI: 10.1002/cjp2.192</identifier><identifier>PMID: 33481339</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Adenocarcinoma ; Antigens, CD - genetics ; Antigens, CD - metabolism ; Antigens, Differentiation, Myelomonocytic - genetics ; Antigens, Differentiation, Myelomonocytic - metabolism ; Apoptosis ; B7-H1 Antigen - genetics ; B7-H1 Antigen - metabolism ; Biomarkers ; Biomarkers - metabolism ; Cancer therapies ; Carcinoma, Pancreatic Ductal - diagnosis ; Carcinoma, Pancreatic Ductal - pathology ; CD163 antigen ; CD20 antigen ; CD3 antigen ; CD4 antigen ; CD4-Positive T-Lymphocytes - immunology ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; Consent ; Disease-Free Survival ; Ethics ; Foxp3 protein ; Gene expression ; Humans ; immune infiltration ; Immunohistochemistry ; Infiltration ; Lymphocytes ; Lymphocytes T ; Medical prognosis ; Meta-analysis ; Pancreas ; Pancreatic cancer ; Pancreatic Neoplasms ; Pancreatic Neoplasms - diagnosis ; Pancreatic Neoplasms - pathology ; PD-L1 protein ; Prognosis ; prognostic biomarker ; Receptors, Cell Surface - genetics ; Receptors, Cell Surface - metabolism ; Reproducibility of Results ; Review ; Systematic review</subject><ispartof>The journal of pathology. Clinical research, 2021-03, Vol.7 (2), p.99-112</ispartof><rights>2021 The Authors. published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd.</rights><rights>2021 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Clinical research</title><addtitle>J Pathol Clin Res</addtitle><description>Immune cell infiltration has been identified as a prognostic biomarker in several cancers. However, no immune based biomarker has yet been validated for use in pancreatic ductal adenocarcinoma (PDAC). We undertook a systematic review and meta‐analysis of immune cell infiltration, measured by immunohistochemistry (IHC), as a prognostic biomarker in PDAC. All other IHC prognostic biomarkers in PDAC were also summarised. MEDLINE, EMBASE and Web of Science were searched between 1998 and 2018. Studies investigating IHC biomarkers and prognosis in PDAC were included. REMARK score and Newcastle–Ottawa scale were used for qualitative analysis. Random‐effects meta‐analyses were used to pool results, where possible. Twenty‐six articles studied immune cell infiltration IHC biomarkers and PDAC prognosis. Meta‐analysis found high infiltration with CD4 (hazard ratio [HR] = 0.65, 95% confidence interval [CI] = 0.51–0.83.) and CD8 (HR = 0.68, 95% CI = 0.55–0.84.) T‐lymphocytes associated with better disease‐free survival. Reduced overall survival was associated with high CD163 (HR = 1.62, 95% CI = 1.03–2.56). Infiltration of CD3, CD20, FoxP3 and CD68 cells, and PD‐L1 expression was not prognostic. In total, 708 prognostic biomarkers were identified in 1101 studies. In summary, high CD4 and CD8 infiltration are associated with better disease‐free survival in PDAC. Increased CD163 is adversely prognostic. Despite the publication of 708 IHC prognostic biomarkers in PDAC, none has been validated for clinical use. Further research should focus on reproducibility of prognostic biomarkers in PDAC in order to achieve this.</description><subject>Adenocarcinoma</subject><subject>Antigens, CD - genetics</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, Myelomonocytic - genetics</subject><subject>Antigens, Differentiation, Myelomonocytic - metabolism</subject><subject>Apoptosis</subject><subject>B7-H1 Antigen - genetics</subject><subject>B7-H1 Antigen - metabolism</subject><subject>Biomarkers</subject><subject>Biomarkers - metabolism</subject><subject>Cancer therapies</subject><subject>Carcinoma, Pancreatic Ductal - diagnosis</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>CD163 antigen</subject><subject>CD20 antigen</subject><subject>CD3 antigen</subject><subject>CD4 antigen</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Consent</subject><subject>Disease-Free Survival</subject><subject>Ethics</subject><subject>Foxp3 protein</subject><subject>Gene expression</subject><subject>Humans</subject><subject>immune infiltration</subject><subject>Immunohistochemistry</subject><subject>Infiltration</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Medical prognosis</subject><subject>Meta-analysis</subject><subject>Pancreas</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>PD-L1 protein</subject><subject>Prognosis</subject><subject>prognostic biomarker</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Reproducibility of Results</subject><subject>Review</subject><subject>Systematic review</subject><issn>2056-4538</issn><issn>2056-4538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1ks1qFEEQxwdRTIgBn0AavHjZ2F_z0R4EWfxYCehBz01Nd83a60z32j2TsAfBR_AZ8yTp2Y0xETx10fXjR1XxL4qnjJ4xSvlLs9nyM6b4g-KY07JayFI0D-_UR8VpShtKKSsZrbl8XBwJIRsmhDoufq6GYfJIDPY9cb5z_RhhxEQgkW0Max_S6AxpXRggfseYMkS24E1EmBt2MiP0BCz6YCAa5zP4igBJuzTisGciXji8JOAtGXCEq1-_wUO_Sy49KR510Cc8vXlPiq_v3n5Zflicf3q_Wr45X5iyZnxhFPKS8pYLaFvVGZv3kJwq2ommksYaaWthDOvKVjFbQiNsDa20XFWWWtuIk2J18NoAG72NLi-z0wGc3n-EuNYQ86g9ajAgTFepqhOVlCjahrUVNqY1UEm0mF2vD67t1A5oDfp8sf6e9H7Hu296HS503VRKCZYFL24EMfyYMI16cGm-P3gMU9JcNlTQshEio8__QTdhivl4e6pmUqlK_BWaGFKK2N0Ow6ieI6LniOgckYw-uzv8LfgnEBlYHIBL1-PuvyK9_PiZz8JrBU_JjA</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>McGuigan, Andrew J</creator><creator>Coleman, Helen G</creator><creator>McCain, R Stephen</creator><creator>Kelly, Paul J</creator><creator>Johnston, David I</creator><creator>Taylor, Mark A</creator><creator>Turkington, Richard C</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5097-5063</orcidid><orcidid>https://orcid.org/0000-0003-3164-1890</orcidid><orcidid>https://orcid.org/0000-0003-4872-7877</orcidid><orcidid>https://orcid.org/0000-0001-5357-1622</orcidid></search><sort><creationdate>202103</creationdate><title>Immune cell infiltrates as prognostic biomarkers in pancreatic ductal adenocarcinoma: a systematic review and meta‐analysis</title><author>McGuigan, Andrew J ; Coleman, Helen G ; McCain, R Stephen ; Kelly, Paul J ; Johnston, David I ; Taylor, Mark A ; Turkington, Richard C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5712-c9e2502b23abb9fcd10742090f3864cdc4d73cc1f5b91d5a83d7ab4d296d0dd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma</topic><topic>Antigens, CD - genetics</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, Myelomonocytic - genetics</topic><topic>Antigens, Differentiation, Myelomonocytic - metabolism</topic><topic>Apoptosis</topic><topic>B7-H1 Antigen - genetics</topic><topic>B7-H1 Antigen - metabolism</topic><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Cancer therapies</topic><topic>Carcinoma, Pancreatic Ductal - diagnosis</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>CD163 antigen</topic><topic>CD20 antigen</topic><topic>CD3 antigen</topic><topic>CD4 antigen</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Consent</topic><topic>Disease-Free Survival</topic><topic>Ethics</topic><topic>Foxp3 protein</topic><topic>Gene expression</topic><topic>Humans</topic><topic>immune infiltration</topic><topic>Immunohistochemistry</topic><topic>Infiltration</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Medical prognosis</topic><topic>Meta-analysis</topic><topic>Pancreas</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - diagnosis</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>PD-L1 protein</topic><topic>Prognosis</topic><topic>prognostic biomarker</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Reproducibility of Results</topic><topic>Review</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McGuigan, Andrew J</creatorcontrib><creatorcontrib>Coleman, Helen G</creatorcontrib><creatorcontrib>McCain, R Stephen</creatorcontrib><creatorcontrib>Kelly, Paul J</creatorcontrib><creatorcontrib>Johnston, David I</creatorcontrib><creatorcontrib>Taylor, Mark A</creatorcontrib><creatorcontrib>Turkington, Richard C</creatorcontrib><collection>Wiley-Blackwell Open Access Titles(OpenAccess)</collection><collection>Wiley Online Library Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>The journal of pathology. Clinical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McGuigan, Andrew J</au><au>Coleman, Helen G</au><au>McCain, R Stephen</au><au>Kelly, Paul J</au><au>Johnston, David I</au><au>Taylor, Mark A</au><au>Turkington, Richard C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune cell infiltrates as prognostic biomarkers in pancreatic ductal adenocarcinoma: a systematic review and meta‐analysis</atitle><jtitle>The journal of pathology. Clinical research</jtitle><addtitle>J Pathol Clin Res</addtitle><date>2021-03</date><risdate>2021</risdate><volume>7</volume><issue>2</issue><spage>99</spage><epage>112</epage><pages>99-112</pages><issn>2056-4538</issn><eissn>2056-4538</eissn><abstract>Immune cell infiltration has been identified as a prognostic biomarker in several cancers. However, no immune based biomarker has yet been validated for use in pancreatic ductal adenocarcinoma (PDAC). We undertook a systematic review and meta‐analysis of immune cell infiltration, measured by immunohistochemistry (IHC), as a prognostic biomarker in PDAC. All other IHC prognostic biomarkers in PDAC were also summarised. MEDLINE, EMBASE and Web of Science were searched between 1998 and 2018. Studies investigating IHC biomarkers and prognosis in PDAC were included. REMARK score and Newcastle–Ottawa scale were used for qualitative analysis. Random‐effects meta‐analyses were used to pool results, where possible. Twenty‐six articles studied immune cell infiltration IHC biomarkers and PDAC prognosis. Meta‐analysis found high infiltration with CD4 (hazard ratio [HR] = 0.65, 95% confidence interval [CI] = 0.51–0.83.) and CD8 (HR = 0.68, 95% CI = 0.55–0.84.) T‐lymphocytes associated with better disease‐free survival. Reduced overall survival was associated with high CD163 (HR = 1.62, 95% CI = 1.03–2.56). Infiltration of CD3, CD20, FoxP3 and CD68 cells, and PD‐L1 expression was not prognostic. In total, 708 prognostic biomarkers were identified in 1101 studies. In summary, high CD4 and CD8 infiltration are associated with better disease‐free survival in PDAC. Increased CD163 is adversely prognostic. Despite the publication of 708 IHC prognostic biomarkers in PDAC, none has been validated for clinical use. Further research should focus on reproducibility of prognostic biomarkers in PDAC in order to achieve this.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33481339</pmid><doi>10.1002/cjp2.192</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-5097-5063</orcidid><orcidid>https://orcid.org/0000-0003-3164-1890</orcidid><orcidid>https://orcid.org/0000-0003-4872-7877</orcidid><orcidid>https://orcid.org/0000-0001-5357-1622</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma Antigens, CD - genetics Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - genetics Antigens, Differentiation, Myelomonocytic - metabolism Apoptosis B7-H1 Antigen - genetics B7-H1 Antigen - metabolism Biomarkers Biomarkers - metabolism Cancer therapies Carcinoma, Pancreatic Ductal - diagnosis Carcinoma, Pancreatic Ductal - pathology CD163 antigen CD20 antigen CD3 antigen CD4 antigen CD4-Positive T-Lymphocytes - immunology CD8 antigen CD8-Positive T-Lymphocytes - immunology Consent Disease-Free Survival Ethics Foxp3 protein Gene expression Humans immune infiltration Immunohistochemistry Infiltration Lymphocytes Lymphocytes T Medical prognosis Meta-analysis Pancreas Pancreatic cancer Pancreatic Neoplasms Pancreatic Neoplasms - diagnosis Pancreatic Neoplasms - pathology PD-L1 protein Prognosis prognostic biomarker Receptors, Cell Surface - genetics Receptors, Cell Surface - metabolism Reproducibility of Results Review Systematic review |
title | Immune cell infiltrates as prognostic biomarkers in pancreatic ductal adenocarcinoma: a systematic review and meta‐analysis |
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